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本病首先由Bourneville(1880)和Pring e(1890)报告,为母斑病中的一型。临床特征有①身体皮肤发生皮脂腺瘤和血管纤维瘤。②癫痫发作。③智能低下。④颅内出现钙化,视网膜及其它脏器出现胶质组织错构瘤等。一般认为本病为不规则染色体显性遗传疾病。笔者最近在临床上发现1例由本病引起左眼球内大出血的病例,比较少见。特报告如下: 患者吴×男24岁安徽籍未婚主诉:左眼视力突然下降2月余。现病史:患者于1989年10月22日无明显诱因,左眼突然视物障碍,无眼痛胀,即去当地医院
The disease was first reported by Bourneville (1880) and Pring e (1890) as one of the motoneurons. Clinical features ① body skin occurs sebaceous tumors and vascular fibroids. ② seizures. ③ smart low. ④ intracranial calcification, retinal and other organs appear glial hamartoma and so on. Generally believed that the disease is irregular chromosomal dominant genetic disease. The author recently found in a clinical case of left eye caused by bleeding in the case of this eye is relatively rare. Special report is as follows: Patient Wu × male 24-year-old Anhui nationality unmarried Complaint: Left eye vision suddenly dropped more than 2 months. Current medical history: patients in October 22, 1989 no obvious incentive, the left eye suddenly sight disorder, no eye swelling, go to the local hospital